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Mingjie Zhang

Researcher at Hong Kong University of Science and Technology

Publications -  312
Citations -  13951

Mingjie Zhang is an academic researcher from Hong Kong University of Science and Technology. The author has contributed to research in topics: PDZ domain & Postsynaptic density. The author has an hindex of 63, co-authored 264 publications receiving 11646 citations. Previous affiliations of Mingjie Zhang include Academia Sinica & Wuhan University of Technology.

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Calcium-induced conformational transition revealed by the solution structure of apo calmodulin.

TL;DR: The solution structure of Ca2-free calmodulin has been determined by NMR spectroscopy, and is compared to the previously reported structure of the Ca2+-saturated form, and concerted movements of helices A and D with respect to B and C, are likely responsible for the cooperative Ca2+,binding property observed between two adjacent EF-hand sites in the amino- and carboxy-terminal domains.
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Phase Transition in Postsynaptic Densities Underlies Formation of Synaptic Complexes and Synaptic Plasticity.

TL;DR: It is discovered that SynGAP, one of the most abundant PSD proteins and a Ras/Rap GTPase activator, forms a homo-trimer and binds to multiple copies of PSD-95, which induces phase separation and forms highly concentrated liquid-like droplets reminiscent of the PSD.
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Organization and dynamics of PDZ-domain-related supramodules in the postsynaptic density.

TL;DR: As the major components of the postsynaptic density of excitatory neuronal synapses, PDZ-domain-containing scaffold proteins regulate the clustering of surface glutamate receptors, organize synaptic signalling complexes, participate in the dynamic trafficking of receptors and ion channels, and coordinate cytoskeletal dynamics.
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Reconstituted Postsynaptic Density as a Molecular Platform for Understanding Synapse Formation and Plasticity.

TL;DR: A biochemical reconstitution approach is used to show that, both in solution and on supported membrane bilayers, multivalent interaction networks formed by major excitatory postsynaptic density (PSD) scaffold proteins led to formation of PSD-like assemblies via phase separation.